Author:
Barnes David J.,Dutton Peter,Bruland Øyvind,Gelderblom Hans,Faleti Ade,Bühnemann Claudia,van Maldegem Annemiek,Johnson Hannah,Poulton Lisa,Love Sharon,Tiemeier Gesa,van Beelen Els,Herbschleb Karin,Haddon Caroline,Billingham Lucinda,Bradley Kevin,Ferrari Stefano,Palmerini Emanuela,Picci Piero,Dirksen Uta,Strauss Sandra J.,Hogendoorn Pancras C. W.,Buddingh Emmeline,Blay Jean-Yves,Cleton-Jansen Anne Marie,Hassan Andrew Bassim
Abstract
AbstractThe phase III clinical study of adjuvant liposomal muramyl tripeptide (MTP-PE) in resected high-grade osteosarcoma (OS) documented positive results that have been translated into regulatory approval, supporting initial promise for innate immune therapies in OS. There remains, however, no new approved treatment such as MTP-PE for either metastatic or recurrent OS. Whilst the addition of different agents, including liposomal MTP-PE, to surgery for metastatic or recurrent high-grade osteosarcoma has tried to improve response rates, a mechanistic hiatus exists in terms of a detailed understanding the therapeutic strategies required in advanced disease. Here we report a Bayesian designed multi-arm, multi-centre, open-label phase II study with randomisation in patients with metastatic and/or recurrent OS, designed to investigate how patients with OS might respond to liposomal MTP-PE, either given alone or in combination with ifosfamide. Despite the trial closing because of poor recruitment within the allocated funding period, with no objective responses in eight patients, we report the design and feasibility outcomes for patients registered into the trial. We demonstrate the feasibility of the Bayesian design, European collaboration, tissue collection with genomic analysis and serum cytokine characterisation. Further mechanistic investigation of liposomal MTP-PE alone and in combination with other agents remains warranted in metastatic OS.
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics,Oncology
Cited by
6 articles.
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